Priority order of neonatal colonization by a probiotic or pathogenic Escherichia coli strain dictates the host response to experimental colitis

The alarming prevalence of inflammatory bowel disease (IBD) in early childhood is associated with imbalances in the microbiome, the immune response, and environmental factors. Some pathogenic Escherichia coli (E. coli) strains have been found in IBD patients, where they may influence disease progression. Therefore, the discovery of new harmful bacterial strains that have the potential to drive the inflammatory response is of great importance. In this study, we compared the immunomodulatory properties of two E. coli strains of serotype O6: the probiotic E. coli Nissle 1917 and the uropathogenic E. coli O6:K13:H1. Using the epithelial Caco-2 cell line, we investigated the different abilities of the strains to adhere to and invade epithelial cells. We confirmed the potential of E. coli Nissle 1917 to modulate the Th1 immune response in a specific manner in an in vitro setting by stimulating mouse bone marrow-derived dendritic cells (BM-DCs). In gnotobiotic in vivo experiments, we demonstrated that neonatal colonization with E. coli Nissle 1917 achieves a stable high concentration in the intestine and protects mice from the progressive effect of E. coli O6:K13:H1 in developing ulcerative colitis in an experimental model. In contrast, a single-dose treatment with E. coli Nissle 1917 is ineffective in achieving such high concentrations and does not protect against DSS-induced ulcerative colitis in mice neonatally colonized with pathobiont E. coli O6:K13:H1. Despite the stable coexistence of both E. coli strains in the intestinal environment of the mice, we demonstrated a beneficial competitive interaction between the early colonizing E. coli Nissle 1917 and the late-arriving strain O6:K13:H1, suggesting its anti-inflammatory potential for the host. This study highlights the importance of the sequence of bacterial colonization, which influences the development of the immune response in the host gut and potentially impacts future quality of life.

The alarming prevalence of inflammatory bowel disease (IBD) in early childhood is associated with imbalances in the microbiome, the immune response, and environmental factors.Some pathogenic Escherichia coli (E.coli) strains have been found in IBD patients, where they may influence disease progression.Therefore, the discovery of new harmful bacterial strains that have the potential to drive the inflammatory response is of great importance.In this study, we compared the immunomodulatory properties of two E. coli strains of serotype O : the probiotic E. coli Nissle and the uropathogenic E. coli O :K :H .Using the epithelial Caco-cell line, we investigated the di erent abilities of the strains to adhere to and invade epithelial cells.We confirmed the potential of E. coli Nissle to modulate the Th immune response in a specific manner in an in vitro setting by stimulating mouse bone marrow-derived dendritic cells (BM-DCs).In gnotobiotic in vivo experiments, we demonstrated that neonatal colonization with E. coli Nissle achieves a stable high concentration in the intestine and protects mice from the progressive e ect of E. coli O :K :H in developing ulcerative colitis in an experimental model.In contrast, a singledose treatment with E. coli Nissle is ine ective in achieving such high concentrations and does not protect against DSS-induced ulcerative colitis in mice neonatally colonized with pathobiont E. coli O :K :H .Despite the stable coexistence of both E. coli strains in the intestinal environment of the mice, we demonstrated a beneficial competitive interaction between the early colonizing E. coli Nissle and the late-arriving strain O :K :H , suggesting its antiinflammatory potential for the host.This study highlights the importance of the sequence of bacterial colonization, which influences the development of the immune response in the host gut and potentially impacts future quality of life.

Introduction
The mucosal surfaces of newborns, including the gastrointestinal tract, undergo dynamic adaptation to the microbial world during the first stages of life, with bacteria playing a dominant role.The first colonizing microbiota educates the immune system, and the nature and order of these bacteria are considered crucial for future health, with long-term consequences for the host (Gensollen et al., 2016).Early-arriving microbes exhibit enhanced colonization stability and have the most significant influence on the microbial community, suggesting that the timing of bacterial arrival in the gut is key to shaping the gut microbiome (Martínez et al., 2018).
The outcome of competitive interactions between arriving microorganisms (coexistence or exclusion of competition) also determines the order in which species arrive in an ecosystem, leading to a phenomenon known as the "priority effect" (Fukami, 2015;Sprockett et al., 2018).Priority effects occur in the gut when: (i) the first colonizing species either occupy or modify the ecological niche (e.g., consume certain nutrients), inhibiting or facilitating later arriving species; (ii) late arriving species have high environmental requirements; or (iii) early and late-arriving species have a strong niche overlap (e.g., closely related taxa and/or taxa competing for the same resources).
Priority effects have been described in the gut ecosystem of gnotobiotic mouse models with isogenic bacterial strains of Bacteroides or Akkermansia species (Lee et al., 2013;Segura Munoz et al., 2022) or mouse fecal communities (Martínez et al., 2018).These ecological principles have also been demonstrated in the establishment of the intestinal microbiome in hospital-associated preterm infants (Rao et al., 2021).However, the specific impact of isogenic bacterial strains of the same species on the host immune response in intestinal inflammation has not yet been investigated.
Inflammatory bowel diseases (IBD) encompass a group of chronic, non-specific, recurrent, immune-mediated inflammations of the gastrointestinal tract.These are divided into similar yet distinct subtypes: Crohn's disease (CD), pouchitis, and ulcerative colitis (UC) (Sartor and Muehlbauer, 2007).The incidence of these diseases has increased dramatically in Western and industrialized countries, suggesting a link between modern lifestyles and environmental factors.Notably, the high prevalence of IBD in early childhood has been recently documented (Park et al., 2020).
These diseases have a multifactorial etiology, combining genetic predisposition and environmental factors such as dysbiotic microbiome, poor dietary habits, stress, impaired intestinal epithelial integrity, dysregulated immune response against commensal gut microbes, and other factors (Zhang and Li, 2014).Although the exact molecular mechanisms of pathogenesis are not yet clear, there is a strong consensus that the intestinal microbiota plays a central role in the development of IBD (Nishida et al., 2018).Current research focuses on the dynamic balance between commensal gut bacteria and host defense mechanisms at the intestinal mucosa in the initiation and maintenance of intestinal inflammation.To date, no specific microbe has been shown to cause IBD, although several specific microorganisms have been investigated as potential factors in IBD etiopathogenesis (Damaskos and Kolios, 2008).
Interestingly, recent research has shown both a decreased diversity of the microbiota and an increased frequency of virulence markers primarily associated with E. coli in IBD (Martinez-Medina and Garcia-Gil, 2014;Moustafa et al., 2018).The majority of IBD patients have been shown to exhibit increased positive antibody responses to a variety of E. coli O antigens, including serotypes O1, O2, O6, O18, and O75.These strains have mostly been associated with urinary tract infections and/or originate from the fecal microbiota (Tabaqchali et al., 1978;Petersen et al., 2009;Mirsepasi-Lauridsen et al., 2019).Epithelial-associated invasive E. coli strains have been frequently isolated from the ileal and colonic mucosa of CD patients, where they can proliferate and damage the host tissue (Boudeau et al., 1999).Mirsepasi-Lauridsen et al. (2016) showed that UC-associated E. coli p19A, an extraintestinal pathogenic E. coli (ExPEC) strain containing α-hemolysin, disrupts the tight junction (TJ) protein occludin in Caco-2 cells in vitro, resulting in increased barrier permeability.In addition, the UC-associated strain p19A induces cell death in dendritic cells and stimulates the release of the proinflammatory cytokines TNF-α, IL-6, and IL-23 (Jensen et al., 2015).
New and emerging therapies for IBD are currently being researched and developed to target immunoregulatory processes.Probiotics and their metabolites are crucial for gut homeostasis, suggesting that they may play a role in the treatment of IBD (Yoshimatsu et al., 2021).
E. coli Nissle 1917 (EcN; O6:K5:H1) is probably the beststudied probiotic strain.It was originally isolated by Alfred Nissle during the First World War in search of wild E. coli strains with antagonistic activity against enteric pathogens (Sonnenborn, 2016).Based on genome analysis, it is currently known that this probiotic strain lacks several defined virulence factors (e.g., α-hemolysin, P-fimbrial adhesins, and the semi-rough lipopolysaccharide phenotype) and expresses fitness factors such as microcins, various iron uptake systems, adhesins, and proteases (Grozdanov et al., 2004).Schlee et al. (2007) showed that E. coli Nissle 1917 induces the expression of human β-defensin 2, an antimicrobial peptide that contributes to the strengthening of the intestinal mucosal barrier by limiting bacterial adherence and bacterial invasion of the gut mucosa.
EcN also strengthens the intestinal epithelial barrier by supporting tight junctions (TJs) between intestinal epithelial cells and modulating the host immune response toward an antiinflammatory balance (Zyrek et al., 2007;Trebichavsky et al., 2010).Several clinical studies have highlighted its remarkable therapeutic effects, especially in maintenance of remission in UC patients (Schultz, 2008).Similarly, the anti-inflammatory effect of this probiotic on the gut has been demonstrated in some experimental colitis models or during the recovery phase from induced colitis in mice and rats (Grabig et al., 2006;Souza et al., 2016;Rodríguez-Nogales et al., 2018;Lu et al., 2019;Park et al., 2021).
In our previous study, we showed that BALB/c mice monocolonized with the probiotic strain E. coli Nissle 1917 did not develop dextran sulfate sodium (DSS)-induced colitis compared to mice monocolonized with the uropathogenic strain E. coli O6:K13:H1, which developed similar inflammatory changes as conventionally reared mice (Hudcovic et al., 2007).Interestingly, we found that the two strains, E. coli Nissle 1917 (O6:K5:H1) and E. coli O6:K13:H1, induce an almost identical gene signature in the small intestine or organoids of monocolonized mice (Janeckova et al., 2019).
In the present study, we focus on the comparative analysis of the immunomodulatory properties of these two strains using in vitro and in vivo experiments.Using the epithelial Caco-2 cell line, we investigated the different abilities of the strains to adhere to and invade epithelial cells.Additionally, using dendritic cells isolated from the bone marrow of mice, we confirmed the potential of E. coli Nissle 1917 to modulate Th1 immune responses.
In gnotobiotic in vivo experiments, we demonstrated that neonatal colonization with E. coli Nissle 1917 induces colonization resistance against E. coli O6:K13:H1 and protects mice against the development of experimentally induced intestinal inflammation.Conversely, in mice neonatally colonized with the pathobiont E. coli O6:K13:H1, a single administration of E. coli Nissle 1917 was inefficient in achieving a high concentration in the intestine, as observed with neonatal colonization, and it did not protect the mice from developing acute ulcerative colitis, demonstrating the absolute importance of the order in which intestinal colonizing strains are introduced.

Bacterial strains
The E. coli Nissle 1917 (EcN; O6:K5:H1) strain was purchased as the probiotic drug Mutaflor (Ardeypharm, Herdecke, Germany).The E. coli O6:K13:H1 (EcO) was originally isolated from the urine of a patient with cystitis and was kindly provided by Prof. L. A. Hanson (Department of Immunology, Institute of Medical Microbiology, University of Gothenburg, Sweden).For in vitro adhesivity and invasivity analysis, the adherent-invasive E. coli LF82 strain (a gift from Arlette Darfeuille-Michaud, France) was used as the positive control (Boudeau et al., 2003).

Bacteria preparation
All E. coli strains were cultivated in Luria-Bertani (LB) broth (Himedia Laboratories, USA) overnight at 37 • C under aerobic conditions.For in vitro adhesivity and invasivity assays on the Caco-2 cell line, a concentration of 2 x 10 7 CFU/ml in PBS was used.
Formalin-inactivated bacteria were used for in vitro stimulation of human embryonic kidney cells and bone marrow-derived dendritic cells (BM-DCs), as previously described (Srutkova et al., 2015).Briefly, bacterial cells were plated on LB agar (Himedia Laboratories, USA) to determine the concentration of the bacterial suspension before inactivation.Bacteria were then centrifuged, washed with phosphate-buffer saline (PBS), and inactivated with 1% formalin in phosphate-buffer for 3 h at room temperature.After inactivation, cells were centrifuged, washed three times with PBS, adjusted to 1 x 10 9 CFU/ml in PBS, and stored at 4 • C.
For the in vivo study, EcN or EcO strains were cultivated overnight in LB broth at 37 • C under aerobic conditions, centrifuged (4000 RPM for 10 min at 4 • C), and diluted in PBS according to optical density to an approximate concentration of 0.5-1.0x 10 9 CFU/ml.The final E. coli concentration administered to the mice was determined by bacteria plating on LB agar as 1.9 x 10 8 CFU/0.2 ml for EcN and 1.1 x 10 8 CFU/0.2 ml for EcO, respectively.

Scanning electron microscopy (SEM)
EcN and EcO strains grown in 5 ml of LB broth at 37 • C overnight were processed as follows: The bacteria were fixed in 3% glutaraldehyde with cacodylate buffer for 15 min at room temperature, followed by overnight incubation at 4 • C. The extensively washed cells were sedimented overnight onto poly-L-lysine-treated circular coverslips at 4 • C. The coverslips with the bacteria were then post-fixed in 1% OsO 4 for 1 h at room temperature.

Transmission electron microscopy (TEM)
The EcN and EcO strains were grown in 5 ml of LB broth at 37 • C until the exponential phase for 3 h.Then, the bacteria were negatively stained on glow-discharge-activated formvar/carbon grids (Benada and Pokorny, 1990) with 1% ammonium molybdate supplemented with 0.1% trehalose (Harris and Scheffler, 2002).The final samples were viewed in a Philips CM100 electron microscope (FEI, formerly Philips EO, The Netherlands) at 80 kV.Digital images were recorded using a Veleta slow-scan camera (EMSis, Muenster, Germany) at a magnification of 25,000× or 46,000× and processed with AnalySis 5.2 software (Olympus Soft Imaging Solutions GmbH, Muenster, Germany).

Caco-cell line culture
The human epithelial colorectal adenocarcinoma cell line (Caco-2) was kindly provided by Zuzana Jiraskova Zakostelska (Institute of Microbiology of the Czech Academy of Sciences).Cells were cultured in Dulbecco's Modified Eagles high glucose, supplemented with 10% fetal calf serum (FCS), 0.01 M HEPES, 1% penicillin/streptomycin, 1% non-essential amino acids, and 2 mM L-glutamine (all Sigma-Aldrich, CO., St. Louis, USA).The cells were routinely cultured in a 75 cm 2 tissue culture flask (Techno Plastic, Trasadingen, Switzerland) at 37 • C in a humidified atmosphere with 5% CO 2 .The medium was changed every second or third day, and cells were re-seeded with trypsin (Sigma-Aldrich, CO., St. Louis, USA) when the monolayer reached 80% confluence.The cell line between the 25th and 30th passages was used for analysis.

Adhesive and invasive properties of E. coli strains determined by transwell culture of the Caco-cell line
Caco-2 cells at a concentration of 2 x 10 4 per 100 µl of media were added to the apical chamber, and 500 µl of complete media was added to the basolateral chamber of the transwell insert in a 24-well plate (Corning, Sigma-Aldrich, CO., St. Louis, USA).The cells were cultured for 21 days, with medium changes in both chambers every second or third day.Afterward, the medium was removed, and the cells were washed two times with PBS to remove any remaining antibiotics.
Live bacteria at a concentration of 2 x 10 6 CFU in 100 µl of antibiotic-free medium were added to the apical part, and 500 µl of antibiotic-free medium was added to the basolateral chamber.After 5 h of incubation at 37 • C in a humidified atmosphere with 5% CO 2 , both chambers were washed three times with 2 ml of PBS.
To determine the adhesive properties of the bacteria, 100 µl of 0.1% Triton-X100 (Sigma-Aldrich) was added to the apical chamber, and the cells with adhered bacteria were harvested by pipetting up and down.The cells were then plated onto Petri dishes with LB agar to determine the number of bacteria adhered to the cells.
To detect invasive properties, transwell inserts with invaded bacteria were washed three times with PBS and then incubated with culture media supplemented with 2% penicillin, streptomycin, and gentamycin (all Sigma-Aldrich) to eliminate adhered bacteria.After 1 hour of incubation at 37 • C, the transwell inserts were washed three times using PBS, and the cells were harvested using 100 µl of 0.1% Triton-X100.The cells were plated on LB agar.The results from three independent experiments are pooled and expressed as a percentage of adhered or invaded bacteria from the input bacterial concentrations.

Stimulation of human embryonic kidney cells stably transfected with TLR , TLR /CD -, and NOD
Human embryonic kidney (HEK) 293 cells stably transfected with plasmid carrying human gene TLR4/MD2/CD14 (a gift from Prof. M. Yazdanbakhsh, Leiden, Netherlands), TLR2/CD14-(InvivoGen, USA), or hNOD2 (InvivoGen, USA) were used to test pattern recognition receptor modulatory analysis (Schwarzer et al., 2013).Briefly, cells (2 × 10 5 cells/ml) were cultured in Dulbecco's complete medium (Sigma-Aldrich) supplemented with appropriate antibiotics (Blasticidin and Hygromycin B Gold from Invivogen, USA) in a final volume of 200 ul per well in a 96-well plate, according to the manufacturer's recommendation.Once the cells adhered to the bottom of the well, EcN or EcO at concentrations of 1 x 10 8 , 1 x 10 7 , and 1 x 10 6 CFU/ml were added.
Culture supernatants were harvested after 20 h of stimulation with formalin-inactivated EcN and EcO, and the cytokine level of human interleukin 8 (IL-8) was measured by ELISA according to the manufacturer's recommendation (Invitrogen, Thermo Fisher Scientific, USA).Each experiment was repeated at least four times.

Immunomodulatory properties of EcN and EcO in bone marrow-derived dendritic cells (BM-DCs)
BM-DC were isolated from naïve BALB/c mice (8 weeks old, n = 2) and prepared as previously described (Srutkova et al., 2015).Briefly, bone marrow precursors isolated from femurs and tibias were seeded at 2 × 10 7 cells/ml in RPMI 1640 culture medium (Sigma-Aldrich) containing 10% FBS, penicillin/streptomycin, 0.01 M HEPES, and 20 ng/ml mouse GM-CSF (eBioscience, USA) and incubated for 8 days at 37 • C in an atmosphere with 5% CO 2 .Fresh medium was added on days 3 and 6.Cells were then harvested, diluted to the final concentration of 2 × 10 6 cells/ml, and stimulated with the formalin-inactivated EcN and EcO strains individually or in a mixture (1:1) at a concentration of 2 x 10 7 CFU/ml for 18 h.
For stimulation using subsequently both bacteria, BM-DCs were cultivated with the first bacterial strain (2 x 10 7 CFU/ml) for 5 h at 37 • C in 5% CO 2 , washed with culture medium, and then the second bacterial strain was added and cultured for 13 h.Ultrapure LPS (1 µg/ml; InvivoGen, USA) was used as a positive control; unstimulated cells (medium) served as a negative control.The levels of IL-10 and IL-12p70 were determined using Ready-Set-Go!Kit (eBioscience, USA) according to the manufacturer's instructions.

Animals
Germ-free (GF), E. coli Nissle 1917, or E. coli O6:K13:H1 monocolonized and experimental groups of BALB/c mice were kept under sterile conditions in Trexler-type plastic isolators in a room with a 12 h light-dark cycle at 22 • C.They were fed a 50 kG irradiated sterile pellet diet (Altromin, Lage, Germany) and provided with sterile drinking water ad libitum.
Sterility and colonization status were controlled every 2 weeks by confirming the absence of unwanted bacteria, molds, and yeasts through aerobic and anaerobic cultivation of mouse feces and swabs from the isolators in VL (Viande-Levure), Sabourauddextrose, and meat-peptone broth, followed by plating on blood, Sabouraud, and VL agar plates.
Specific pathogen-free (SPF) mice were kept in individually ventilated cages (IVC) (Tecniplast S.P.A., Italy), with a 12 h lightdark cycle at 22 • C, fed a 25 kG irradiated sterile pellet diet (Altromin, Lage, Germany), and provided with drinking water ad libitum.SPF mice were regularly checked for the absence of potential pathogens according to an internationally established standard (FELASA).Animal experiments were approved by the committee for the protection and use of experimental animals at the Institute of Microbiology of the Czech Academy of Science (approval ID: 18/2019).

Experimental design
Germ-free (GF) mice were colonized by intragastric gavage with either E. coli Nissle 1917 (Mutaflor) or E. coli O6:K13:H1, and mated after a 2-week colonization period.Their offspring were used for in vivo studies.
Subsequently, 2-month-old female offspring were divided into experimental groups according to bacterial colonization and DSScolitis induction: After 15 days of the second colonization, mice received autoclaved 2.5% w/v dextran sulfate sodium (DSS, M.W. 36-50 kDa; MP Biomedicals, Illkirch, France) in drinking water ad libitum for 7 consecutive days to induce acute colitis (see Figure 1, experimental design).Mice colonized by EcN+EcO or EcO + EcN without DSS-induced colitis served as healthy controls.The experiment was repeated three times.To ensure the efficiency of the 2.5% DSS solution, 8-10 weeks-old BALB/c mice reared in SPF conditions were used as a positive control for acute intestinal inflammation, where signs of inflammation such as rectal bleeding and weight loss were apparent (data not shown).At the end of the experiment, occult bleeding was evaluated in stool samples using the hemocult test (Hemocare, Care Diagnostic GmbH, Austria) and scored as follows: • 0: No visible bleeding, hemocult negative.
After sacrifice colon were aseptically removed, its length measured, and tissue segments fixed in Carnoy's fluid for 30 min, transferred into 96% ethanol, and embedded in paraffin.

Histological evaluation of inflammation in the colon
Paraffin-embedded sections (5 µm) were cut and stained with hematoxylin and eosin (H&E) or Alcian Blue/Nuclear Fast Red (all from Vector Labs, Burlingame, USA) for mucin production.The samples were viewed under an Olympus BX 40 microscope equipped with an Olympus Camedia DP 70 digital camera, and the images were analyzed using Olympus DP-Soft.The degree of surface epithelium damage, crypt distortion, and mucin production in individual colon segments was evaluated, and the histopathological score was assessed according to Hudcovic et al. (2001).

Immunohistochemical determination of zonula occludens (ZO)-in colon
Colon-descendent segments were embedded in O.C.T. Tissue-Tek (Sakura Finetek, Alphen aan den Rinj, Netherlands) and frozen in liquid nitrogen.Acetone-fixed cryosections (5 µm thick) were used for immunohistochemistry. Expression of ZO-1 was detected using rabbit anti-mouse polyclonal antibody (Zymed Laboratories, Carlsbad, CA, USA) and secondary antibody Cy3 goat anti-rabbit IgG (Biomeda, Foster City, USA).The samples were viewed under an Olympus BX 40 microscope equipped with an Olympus Camedia DP70 digital camera, and the images were analyzed using Olympus DP-Soft (Jourova et al., 2022).

Detection of E. coli Nissle and E. coli O :K :H by qPCR
Fecal samples were collected 1 day before (day-1) intragastric administration of the second E. coli strain, 12 h after the administration of the second strain (day 0), and on subsequent days throughout the colonization of mice as depicted in the experimental design (Figure 1).Samples were stored at −40 • C for qPCR analysis.A part of the fecal sample was serially diluted with sterile PBS and plated on modified McConkey agar supplemented with 2% raffinose, prepared according to  2014) (see Supplementary materials and methods and Supplementary Figure S2).Total DNA from the feces of colonized mice or pure E. coli Nissle 1917/E.coli O6:K13:H1 culture was isolated using the ZR Fecal DNA Kit according to the manufacturer's instructions (Zymo Research, USA).Agarose gel electrophoresis and UV spectrophotometry confirmed the purity, integrity, and concentration of nucleic acids.
To generate a standard curve for qPCR analysis, bacterial DNA was extracted from 150 µl of 10x diluted fecal samples in PBS (w/v) of monocolonized mice (EcN or EcO).Subsequently, the bacterial concentration (CFU/g of feces) corresponding to 1 µl of isolated DNA was determined by plating on LB agar (Himedia Laboratories, USA) and cultivating aerobically overnight at 37 • C. A five-point standard curve (10-fold dilutions corresponding to 10 6 to 10 2 CFU per 1 µl of DNA) was used for absolute bacterial quantification of E. coli Nissle 1917 or O6:K13:H1 in qPCR reactions.The C T values at the different dilution points were averaged, and the total number of bacterial cells was interpolated from the averaged standard curve as described elsewhere (Ott et al., 2004;Costa et al., 2022).
Amplification and detection were carried out in 96-well optical plates using the Bio-Rad Real-time PCR Detection System iQ5 (Bio-Rad laboratories, USA) in a final volume of 20 µl per reaction containing 1 µl of a 10x diluted sample of DNA, 2x MM Syto9 (Top-Bio, Czechia), a 0.4 µM concentration of each primer, and PCR water.For the detection of E. coli Nissle 1917, primers Muta-9/Muta-10 (forward: 5'gcg agg ta acct cga aca tg 3'; reverse: 5'cgg cgt atc gat aat tca cg 3') according to Blum-Oehler et al. (2003) were used.The quantitative PCR was performed with an initial hold of 95 • C for 3 min, followed by 35 cycles of denaturation at 95 • C for 45 s, annealing at 60 • C for 45 s, and elongation at 72 • C for 45 s, and with a final elongation step at 72 • C for 10 min (Blum-Oehler et al., 2003).
For the amplification of E. coli O6:K13:H1, primers detecting the hlyA gene were used (forward: 5'tca gga act ggt ttg aaa aa 3'; reverse: 5'att acc tgc agc tga aat ga 3') (Sheshko et al., 2006).The quantitative PCR was performed with an initial hold of 95 • C for 5 min, followed by 35 cycles of denaturation at 95 • C for 45 s, annealing at 56 • C for 45 s, and elongation at 72 • C for 45 s, with a final elongation step at 72 • C for 10 min.After each qPCR run, melting curve analysis was performed to verify the presence of the desired amplicon.

Colon fragment cultures
Fragments of the distal colon were washed with PBS to remove fecal contents, weighed, cut to approximately 100 mg each, and cultured in RPMI 1640 supplemented with 100 U/ml penicillin, 100 µg/mL streptomycin, 1% HEPES (all Sigma-Aldrich), and 10% heat-inactivated fetal calf serum at 37 • C, a 5% CO 2 for 48 h.Supernatants were collected and stored at −40 • C until further processing (Hudcovic et al., 2012).The levels of cytokines IL-1β, IL-6, and TNF-α were determined using a Mouse Cytokine/Chemokine Multiplex Immunoassay (Millipore-Sigma, MO, USA) according to the manufacturer's instructions.

Statistical analysis
Data are expressed as mean ± standard error of the mean (SEM).Data were analyzed using the Student's t-test or oneway ANOVA with Tukey's post-hoc test.All statistical analyses were conducted using GraphPad Prism 8.0 Software (San Diego, CA, USA).

Analysis of adhesive and invasive properties of E. coli Nissle and E. coli O :K :H
Scanning (Figures 2A, B) and transmission (Figures 2C,  D, Supplementary Figures S1A, B) electron microscopy were performed on E. coli Nissle 1917 (EcN) and O6:K13:H1 (EcO) cultures to investigate the surface structures of bacterial cells.An overnight culture with elongated bacterial cells in a stationary growing phase was used for scanning electron microscopy analysis.For TEM analysis, a fresh culture of E. coli cells in the exponential phase was used to ensure the fine structures of both flagella and pili.Both strains exhibited regular rod-shaped structures with a mean cell length of approximately 1-2 µm and a mean thickness of approximately 0.8-1.2µm (Supplementary Figure S1C).
Scanning electron microscopy of EcN (Figure 2A) and EcO (Figure 2B) displayed a formed filamentous network with flagella connecting bacterial cells.The transmission electron microscopy analysis (Figures 2C, D, Supplementary Figures S1A, B) confirmed the presence of typical filamentous structures on the surface of strains, including flagella and pili.The long and thicker flagella had an average diameter of 17 ± 2 nm (Supplementary Figure S1D), and the thinner and shorter pili had diameters smaller than 10 nm.The presence of pilli and flagella structures was found on both EcN and EcO, ensuring their potential for adhesion to the epithelial cells in the host or cell cultures.
The ability of EcN and EcO to adhere to and invade epithelial cells was tested using a polarized Caco-2 transwell culture, which mimics the intestinal environment.The adherent/invasive strain Escherichia coli LF82, originally isolated from the ileum of a patient with Crohn's disease and capable of disrupting the apical junctional complexes in polarized epithelia, was used as the positive control (Boudeau et al., 2003;Wine et al., 2009).As expected, E. coli LF82 showed high adhesive and invasive ability in the polarized Caco-2 cell line.
Both analyzed EcN and EcO strains displayed weaker efficiency in adhering to (Figure 2E) and invading epithelial cells compared to the positive control (Figure 2F).Nonetheless, EcO was significantly more adhesive and showed a trend toward higher invasiveness than EcN.These results suggest that EcO, as a uropathogenic strain, has better mechanisms for attaching to the epithelial cells of the host.

Stimulation of human embryonic kidney cells stably transfected with TLR , TLR /CD -and NOD by E. coli Nissle and E. coli O :K :H
HEK 293 cells stably transfected with human genes for pattern recognition receptors TLR4, TLR2/CD14-or NOD2 were used to investigate the innate signaling pathways activated by both E. coli strains.Our results showed that both strains are strongly recognized by TLR4 and TLR2/CD14-receptors in a similar dosedependent manner (Figures 3A, B).There were no differences in signaling through the TLR4 or TLR2/CD14-pathways between the studied strains at the tested bacteria concentrations, suggesting that surface structures such as LPS or lipoproteins are sensed similarly.However, EcO was recognized more intensively by the NOD2 receptor than EcN, suggesting differences in the sensing of peptidoglycan structures (Figure 3C).  ) for h, and after the washing step, the cells were stimulated by the second strain (EcO or EcN, resp.).The cytokines ILand IL-p were determined in cell culture supernatants by ELISA.The results are expressed as the ratio of IL-/lL-p production.The data are pooled from two independent experiments with a total of biological replicates and expressed as the mean ± SEM.A statistical evaluation by t-test was performed for di erences analysis between EcN and EcO stimulation or cultures sequentially stimulated by both EcN and EcO strains (*p < .and **p < .).

Frontiers in Microbiology
frontiersin.orgsecond colonizing bacteria (EcO+EcN+DSS) showed bleeding scores and colon shortening similar to EcO-monocolonized mice after DSS treatment.Histological analysis of the colon mucosa confirmed macroscopic signs of inflammation, indicating that one-dose treatment with EcN is ineffective in preventing DSSinduced intestinal inflammation in EcO-colonized mice.Similar results were observed in adult GF mice colonized by a mixture of EcN and EcO (Supplementary Figures S3C-H), showing moderate signs of inflammation, rectal bleeding, colon shortening, and mild histopathological changes in the colonic mucosa.
Altered intestinal barrier function through decreased expression of tight junction proteins, such as ZO-1, is a critical factor in the development of intestinal inflammation in mouse models of colitis or human IBD.In this study, we investigated whether neonatal EcN colonization or one-dose EcN treatment influenced the alteration of ZO-1 induced by DSS treatment in EcO-colonized mice.Immunohistochemistry staining (IHC) revealed reduced ZO-1 expression after DSS administration in the mice colonized with only EcO, compared to healthy controls.In contrast, preserved ZO-1 expression was evident in both neonatally EcN-colonized and one-dose EcN-treated mice (Figure 5H).
These results demonstrate the priority effect of EcN on the host, showing that EcN neonatal colonization prior to EcO colonization protects the host from the induction of the inflammatory response driven by the pathogenic EcO strain.

Neonatal colonization by E. coli Nissle downregulated the level of proinflammatory cytokines in colon tissue
Changes in the cytokine microenvironment in the gut were analyzed in the supernatants of colon tissue fragment cultures from the mice neonatally colonized by EcN or EcO, co-colonized by EcO or EcN, and treated with 2.5% DSS to induce intestinal inflammation.Similar to macroscopic and histopathological evaluation, the mice monocolonized by EcO and treated by DSS showed a significant upregulation of proinflammatory cytokines IL-1β (Figure 6A), IL-6 (Figure 6B), and TNF-α (Figure 6C) compared to healthy controls without DSS treatment.Notably, we found that neonatal colonization by EcN efficiently protected against the upregulation of these proinflammatory cytokines in DSS-treated mice, even when the potentially pathogenic EcO was administered 2 weeks before colitis induction by DSS.Insignificant downregulation of these cytokines was also observed in mice where EcN was administered as the second colonizing stimulus in one dose only.These results highlight the potential of E. coli Nissle .
1917 to protect against inflammation, even in the presence of the potentially pathogenic E. coli O6:K13:H1 strain.

Discussion
The first year of life is crucial for newborns to develop their commensal microbiota, which influences the development of their immune system and has corresponding consequences for their lifelong health.The neonatal gut is an aerobic environment at birth, where only facultative anaerobes such as Escherichia coli and Enterococcus eventually create a favorable anaerobic environment for colonization by subsequent microbes (Jost et al., 2012;Matamoros et al., 2013).This pioneering microbiome has lifelong effects and shows that colonization in childhood can persist into adulthood, influencing the development of many diseases.These findings suggest that the sequence and type of bacteria that colonize our bodies after birth are of utmost importance for our future health (Faith et al., 2013).
In this study, we compared two related strains of E. coli of serogroup O6: probiotic E. coli Nissle 1917 and uropathogenic E. coli O6:K13:H1, focusing on their ability for neonatal colonization and competitive interaction in the intestinal mucosa, their influence on the development of the immune system, and their effects on the development of intestinal inflammation in adult mice.
Using in vitro experiments, we found that both strains possess distinct properties regarding adhesiveness to Caco-2 epithelial cells and modulation of the Th1 immune response in BM-DC cultures.In gnotobiotic in vivo experiments, we demonstrated that neonatal colonization with E. coli Nissle 1917 confers colonization resistance to E. coli O6:K13:H1 and protects mice from developing experimentally induced intestinal inflammation.
Conversely, in mice neonatally colonized with the pathobiont E. coli O6:K13:H1, one-dose administration of E. coli Nissle 1917 does not reach as high a concentration in the intestine as in the neonatal setup and fails to protect the mice from developing acute ulcerative colitis.These findings highlight the critical importance of the order of arrival of the intestinal colonizing strains.
Finally, we showed that the colonization of adult germ-free mice with a mixture of EcN and EcO strains in a 1:1 ratio (Supplementary Figure S3) had only a weak effect on the alleviation of DSS-induced intestinal inflammation compared to the mice neonatally pre-colonized with EcN strain, where EcO was the second colonizing strain or mice that were mono-colonized only with the EcN strain throughout the entire experiment.These results demonstrate the priority effect of neonatal colonization with E. coli Nissle on the host's immune response to inflammatory stimuli later in life.
Studies in IBD patients have found an increased incidence of E. coli strains that can adhere to and invade epithelial cells vitro (Boudeau et al., 1999).This type of adherent-invasive E. coli strain (also known as AIEC) has specific factors for adherence to intestinal epithelial cells, invasion into the cytoplasm of the infected eukaryotic cells, and intracellular replication in epithelial cells and macrophages, which consequently facilitates the development of IBD in humans (Barnich and Darfeuille-Michaud, 2007).
The impact of neonatal colonization by the LF82 strain (belonging to the AIEC group) together with altered Schaedler microbiota (ASF) in comparison to colonization by LF82 in adult ASF mice was introduced by Wymore Brand et al. (2022).The authors showed that neonatal colonization with LF82 aggravated DSS-induced colitis to a greater extent than when the strain was administered to adult mice.Their results are in line with our study, highlighting the importance of the timing of bacterial strain arrival and its consequences on the host's inflammatory response.
For scientists, it is crucial to search for potentially pathogenic E. coli isolates with properties similar to those possessed by the AIEC strains, as these could be associated with the pathogenesis of IBD.In this context, Martinez-Medina et al. (2009) showed that the uropathogenic strain E. coli OL96a can adhere to and invade the intestinal epithelial cells, shares some virulence genes with AIEC, and is phylogenetically related to intestinal AIEC strains.Similarly, in this study, we investigated E. coli O6:K13:H1 as an extraintestinal strain for its ability to adhere to and invade epithelial cells, modulate immune responses, and induce intestinal inflammation using in vitro and in vivo experiments.
Many pathogenic bacteria bind to the host tissue via adhesive surface organelles called pili, which are important virulence factors for various diseases, especially infections of the urinary, genital, and gastrointestinal tracts.In addition, type 1 pili have been found to be responsible for bacterial invasion and persistence in target cells (Capitani et al., 2006).Using transmission and scanning electron microscopy, we showed that both EcO and EcN strains express sufficient numbers of pili and flagella structures, suggesting their potential for adhesion and invasion into host epithelial cells.
Using transwell cultures, we demonstrated that EcO adheres more strongly to the Caco-2 epithelial cell line than the probiotic EcN strain but approximately 20 times less than the AIEC control strain LF82.
Furthermore, we found that the EcO strain has no invasive activity, indicating that this strain does not belong to the AIEC group.These results are consistent with the fact that uropathogenic E. coli strains should possess the factors that enable better adhesion to epithelial cells, quorum sensing, and biofilm formation, which directly or indirectly contribute to the development of urinary tract infections (Shah et al., 2019).
Epithelial and immune cells can recognize LPS, flagella, and peptidoglycan of E. coli via pattern recognition receptors (PRR).The interaction between TLRs and E. coli cell structures could activate the signaling pathways leading to the production of proinflammatory cytokines such as TNF-α or IL-6.Using HEK 293 cells, we demonstrated that both EcN and EcO strains are strongly recognized by TLR4 and TLR2 receptors in a similar dose-dependent manner.However, EcO was more intensely recognized by NOD2 receptors than EcN, suggesting differences in recognizing peptidoglycan structures.NOD2 variants are associated with Crohn's disease, in which a defect in recognizing commensal bacteria leads to gastrointestinal inflammation (Al Nabhani et al., 2017).An overexpression of NOD2 in Caco-2 cells led to a greater increase in the autophagy process, which was associated with decreased survival of AIEC and the release of proinflammatory cytokines (Negroni et al., 2016).
These results highlight the important role of NOD2 signaling in activating autophagy processes as a host defense mechanism to control the overgrowth of pathogenic bacteria (Al Nabhani et al., 2017).Cooney et al. (2010) have demonstrated that NOD2 signaling is crucial for muramyl dipeptide-induced autophagy in DCs, as well as for subsequent MHC class II upregulation, DC activation, and antigen presentation.In this study, we compared EcN and EcO strains in terms of their ability to activate BM-DCs.Interestingly, the expression of CD40, CD80, and CD86 co-stimulatory surface markers was induced similarly by both strains and was comparable to the LPS control.However, we found that stimulation of BM-DCs with the EcN strain itself induces a higher anti-inflammatory cytokine ratio (IL-10/IL-12p70) than stimulation with the EcO strain.This phenomenon was preserved even when the BM-DC culture was pre-incubated by EcN before adding strain EcO to the culture.
Conversely, this effect was not apparent in BM-DC cultures co-incubated with a mixture of EcN and EcO, nor when EcN was added as the second bacterial stimulus.Our results are in line with the findings by Güttsches et al. (2012), showing that EcN lysate and its LPS induced the same level of IL-12p40 in comparison to the uropathogenic E. coli W536 strain but upregulated IL-10 production in human PBMC cultures.Boudeau et al. (2003) demonstrated a significant inhibitory effect of E. coli Nissle 1917 on the adhesion and invasion of AIEC in intestinal epithelial cell lines.Similarly, Leatham et al. (2009) showed that E. coli Nissle 1917 limits the growth of pathogenic E. coli O157:H7 in the intestine of streptomycintreated mice.In agreement with these results, this study shows that neonatal colonization of germ-free mice with EcN and subsequent administration of uropathogenic EcO allowed the growth of the EcO strain to a lower but stable level compared to the levels of the first colonizing EcN strain.Conversely, the concentration of the EcO strain in neonatally colonized mice never reached the levels of the EcN strain, suggesting an adaptation of the EcO strain to an extraintestinal niche.
The finding that EcO levels remain stable in neonatally colonized mice after the administration of the EcN strain suggests that the effect of EcN is not mediated by competitive exclusion of the pathogenic strain.Despite the stable coexistence of both E. coli strains in the intestinal environment of the mice, we demonstrated a competitive interaction that favors the early colonizing EcN strain over the later colonizing EcO strain.This so-called priority effect was described by Segura Munoz et al. (2022) for strains of Akkermansia muciniphila and Bacteroides vulgatus, in which the competitive ability of the strain has been influenced by the time of arrival.
Of particular importance is our demonstration that the primary effect of the EcN strain implies its anti-inflammatory potential for the host.We demonstrated that neonatal colonization with E. coli Nissle 1917 inhibited the contribution of EcO infection to intestinal inflammation upon DSS treatment.
Conversely, a single treatment with EcN is ineffective in protecting the development of DSS-induced ulcerative colitis in mice neonatally colonized with pathobiont EcO.
Our results are in line with the study by Pradhan and Weiss (2020), who investigated the probiotic properties of the EcN strain in human intestinal organoids (HIOs).They showed that preincubation of HIOs with EcN before they were challenged with EHEC or UPEC prevented the loss of epithelial barrier function, loss of E-cadherin expression, and increased production of reactive oxygen species and apoptosis.They described that EcN did not replicate in HIO co-culture like the pathogenic strains, thus conferring protection via activation of host defenses rather than eliminating competing strains.
Overall, we have described the interaction between two E. coli strains of the same O6 serotype, the uropathogenic O6:K13:H1 and the probiotic Nissle 1917 (O6:K5:H1), with regard to their effects on the host.Given the importance of the first colonizing bacterial strains in developing the immune response, we investigated how the order of arrival of these E. coli strains influences the host's response to inflammatory stimuli and the long-term effects on health.
Our results demonstrate that E. coli Nissle 1917 has the potential to protect against DSS-induced intestinal inflammation, even after co-infection with E. coli strain O6:K13:H1, which has proinflammatory potential.This study emphasizes the importance of a probiotic intervention approach, particularly with the E. coli Nissle strain, during the perinatal/neonatal period to prevent an aberrant microbiome and dysbiosis-related diseases such as IBD in an individual's later life.
Future research should explore additional strains with known niche properties, assess their competition within the broader microbial community, and focus on the precise mechanisms by which strains coexist, compete, and impact host health.

FIGURE
FIGUREExperimental design.BALB/c mice neonatally colonized with E. coli Nissle or E. coli O :K :H were co-colonized by the second E. coli strain at the age of months after birth.Fifteen days after the co-colonization with the second bacteria, intestinal inflammation was induced by .% dextran sodium sulfate (DSS) administration in drinking water for consecutive days.Mice colonized by both E. coli strains without DSS administration served as healthy controls.Fecal samples for qPCR detection of bacteria were collected throughout the whole experiment on the indicated days.

FIGURE
FIGURE In vitro analysis of adhesive and invasive properties of E. coli Nissle and E. coli O :K :H by scanning and transmission electron microscopy and Caco-cell line transwell cultures.Scanning electron microscopy of (A) E. coli Nissle and (B) E. coli O :K :H shows a filamentous network via flagella.Scale bar = µm.Transmission electron microscopy of negatively stained (C) E. coli Nissle and (D) E. coli O :K :H shows flagella (F) and pili (P) structures.Scale bar = µm.Caco--polarized cell monolayers were cultured on transwell inserts for days.Overnight bacterial cultures of E. coli Nissle (EcN), E. coli O :K :H (EcO), and E. coli LF (LF ) were added to the apical part of the insert and left to adhere/invade for h.(E) Adherent bacteria were detected on the surface of intact Caco--polarized cells.(F) Invading bacteria were determined after antibiotic treatment and the removal of bacteria adhered to the surface of Caco-cells.Results are shown as % of adhered or invaded bacteria from bacterial input concentration and expressed as mean ± SEM.The data are pooled from three independent experiments with two to five biological replicates.Each experiment is denoted by a specific symbol (circle, square, and diamond).A Student's t-test was used for comparison between the EcN and EcO groups (**p < .).

FIGURE
FIGURE Stimulation of TLR , TLR /CD -, and NOD receptors by E. coli Nissle and E. coli O :K :H .Human embryonic kidney cells (HEK ) stably transfected with an expression vector for (A) human TLR ( -hTLR /MD /CD ), (B) human TLR ( -hTLR /CD -), or (C) human NOD ( -hNOD ) were stimulated with formalin-inactivated E. coli Nissle (EcN) or E. coli O :K :H (EcO) for h.Stimulation was performed at concentrations of , , or CFU/ml.Cells stimulated with lipopolysaccharide (LPS-EB, µg/ml), PAM CSK (PAM , µg/ml), or muramyl dipeptide (MDP, µg/ml) were used as positive controls.Untreated cells (M) were used as negative controls.The data are pooled from eight experiments performed for TLR analysis, four experiments for TLR /CD -, and six experiments for NOD analysis and expressed as the production of IL-(pg/ml).Each experiment is denoted by a specific symbol with one or two biological replicates for each bacterial concentration.Di erences between EcN and EcO stimulation were statistically evaluated using the t-test (**p < .and *p < .).

FIGUREE
FIGURE E. coli Nissle and E. coli O :K :H strains activate the maturation and cytokine production of BM-DCs.(A) BM-DCs from naïve mice were cultured with formalin-inactivated E. coli Nissle (EcN) and E. coli O :K :H (EcO) for h.Lipopolysaccharide from E. coli (LPS-EB, µg/ml) was used as a positive control.Untreated cells (medium) served as a negative control.The expression of CD , CD , and CD was assessed using flow cytometry.BM-DCs were gated as MHCII + CD c + .Numbers represent the median fluorescence intensity from one representative experiment out of two.(B) BM-DCs were stimulated with formalin-inactivated strains EcN, EcO, and a mixture of EcN and EcO or pre-incubated first with one strain (EcN or EcO, resp.) for h, and after the washing step, the cells were stimulated by the second strain (EcO or EcN, resp.).The cytokines ILand IL-p were determined in cell culture supernatants by ELISA.The results are expressed as the ratio of IL-/lL-p production.The data are pooled from two independent experiments with a total of biological replicates and expressed as the mean ± SEM.A statistical evaluation by t-test was performed for di erences analysis between EcN and EcO stimulation or cultures sequentially stimulated by both EcN and EcO strains (*p < .and **p < .).

FIGURE
FIGURE Neonatal colonization but not one-dose treatment by E. coli Nissle protects against the development of severe colitis in an experimental mouse model.The e ciency of neonatal and second re-colonization by E. coli Nissle (EcN) and E. coli O :K :H (EcO) was detected by qPCR from fecal samples throughout the experiment.(A) Neonatally colonized mice by EcN with one-dose treatment by EcO reached stable, high colonization e ciency of their parenteral E. coli strain.(B) E. coli Nissle was administered in one dose as the second strain to EcO-colonized mice.Stable colonization e ciency was detected by qPCR throughout the whole experiment, using fecal samples.(C) The rectal bleeding score was analyzed in mice neonatally colonized by EcN or EcO, treated with the second strain (EcO or EcN), and with .% DSS to induce acute ulcerative colitis.(D) Shortening of the colon was evaluated in experimental mice on sacrifice day.(E) The histopathological score was determined in colon (Continued)